Jordan Lockwood
Biomedical Consultant, Fda, Hc, Iec, Iso, Eu Mdr, Pmda Japan and Fda
We found the following information about Jordan Lockwood at Philips Respironics, where Jordan has worked as a Post Market Surveillance Mdr Consultant since 2019. Jordan's total work experience is over nine years, during which time the professional had at least 13 jobs at different companies to develop professional skills. Jordan studied at the Grand Canyon University from 2015 to 2019. Jordan can be found in Denver, Colorado – where this expert currently lives. You can search for their contacts. We can also provide you detailed contact information upon request.
Name variants:
Jorden Lockwood,
Jordyn Lockwood
Contact Information
Last Update
Jul 9, 2022
Email
jl**@greatbatchmedical.com
Location
Denver, CO
Company
Workplace
Colleagues
Work History
Post Market Surveillance Mdr Consultant
3 month on Contract as a Consultant in Post Market Surveillance: Complaint Investigations and Medical Device Reporting as a response effort for FDA Compliance.
May 2019 — Jul 2019
Supplier Quality Management Eu Mdr Consultant
345 east Main St #p/o box 708, Warsaw, IN 46580
3 month on Contract as a Supplier Quality Engineer for United States and China. Supplier Management, Technical File Review and CE Mark updates in response to EU MDR.
Apr 2019 — Jun 2019
Senior Consultant
557 Mccormick St, San Leandro, CA 94577
Nov 2018 — Mar 2019
Risk Management Engineering Consultant
1212 Terra Bella Ave, Mountain View, CA 94043
Mar 2017 — May 2017
Quality Engineering Consultant
325 Paramount Dr, Raynham, MA 02767
Risk Management SME, North American & European Tech File Remediation Project. Contracted through Oxford Global Resources
May 2016 — Jan 2017
Quality Systems and Regulatory Affairs, Validation Consultant
1735 Merchants Ct, Colorado Springs, CO 80916
Quality System and Engineering Management Remediation in Preparation for FDA Inspection. Contracted through Black Diamond Networks
Nov 2015 — Jan 2016
Independent Contractor
Professional sabbatical to fill a critical need with my family's real estate company, Lucas Properties Arizona of Lucas Oil Products, Inc.
Dec 2014 — Nov 2015
Regulatory Compliance Consultant: Biologics
56 east Bell Dr, Warsaw, IN 46582
Premarket Approval, 510k, Reclassification Class II to Class III, Biologics. Global Regulatory Affairs & Supplier Quality Consultancy for Validation & Supplier Quality Management System Reme...
Oct 2013 — Aug 2014
Quality Assurance Analyst
Indiana
Premarket Approval, 510k, New Product Development, Combination Products. Global Regulatory Affairs, Validation, & Quality Engineering Consultancy with Cross Functional Collaboration with San...
Oct 2012 — Mar 2013
Metrologist Ii
9825 Kenwood Rd SUITE 302, Cincinnati, OH 45242
Apr 2012 — Oct 2012
Education
2015 — 2019
2007 — 2009
Occupations
Counselor
Sales Specialist
Supplier
Engineer
Quality Engineer
Advisor
Services Professional
Sales Representative
Compliance Engineer
Skills
Medical Devices
Quality System
Iso 13485
Capa
Fda
Quality Assurance
Iso 14971
Design Control
Fmea
Lean Manufacturing
Validation
Continuous Improvement
Microsoft Office
Iso
Supplier Quality
Quality Auditing
Spc
V&V
Minitab
Root Cause Analysis
21 Cfr
Gmp
Iso 9000
Product Launch
Value Stream Mapping
Quality Control
Design of Experiments
Disposables
5S
Injection Molding
Change Control
Process Capability
Process Improvement
Product Development
Ppap
Orthopedic
Apqp
Ts16949
Regulatory Affairs
Fda Gmp
Equipment Qualification
Quality System Compliance
Complaint Investigations